Canonical Allele Identifier: CA2320961350
Gene: MCOLN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7525105A= , CM000681.2:g.7525105A= GRCh38
NC_000019.9:g.7589991A= , CM000681.1:g.7589991A= GRCh37
NC_000019.8:g.7495991A= NCBI36
NG_015806.1:g.7496A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264079.11:c.176A= MANE Select ENSP00000264079.5:p.Lys59=
ENST00000264079.10:c.176A= ENSP00000264079.5:p.Lys59=
ENST00000394321.9:n.256A=
ENST00000596390.1:n.292A=
ENST00000601003.1:c.176A= ENSP00000469074.1:p.Lys59=
NM_020533.2:c.176A= NP_065394.1:p.Lys59=
NM_020533.3:c.176A= MANE Select NP_065394.1:p.Lys59=